Division of Maternal-Fetal Medicine, Department of Obstetrics and Gynecology, University of Utah Health Sciences Center, Salt Lake City, 84132, USA.
Am J Obstet Gynecol. 2011 May;204(5):391.e1-8. doi: 10.1016/j.ajog.2010.09.021. Epub 2010 Nov 11.
We sought to identify serum markers of subsequent spontaneous preterm birth (SPTB) in asymptomatic women prior to labor.
Serum proteomics was applied to sera from 80 pregnant women sampled at 24 weeks and an additional 80 pregnant women sampled at 28 weeks. Half had uncomplicated pregnancies and half had SPTB.
Three specific peptides arising from inter-alpha-trypsin inhibitor heavy chain 4 protein were significantly reduced in women at 24 and 28 weeks having subsequent SPTB. The most discriminating peptide had a sensitivity of 65.0% and specificity of 82.5%; odds ratio, 8.8; and 95% confidence interval, 3.1-24.8. A combination of the 3 new biomarkers and 6 previously studied biomarkers increased sensitivity to 86.5%, with a specificity of 80.6% at 28 weeks.
Three novel serum markers of SPTB have been identified using serum proteomics. Using a combination of these new markers with additional markers, women at risk of SPTB can be identified weeks prior to SPTB.
我们旨在确定分娩前无症状孕妇发生自发性早产(SPTB)的血清标志物。
应用血清蛋白质组学技术对 80 名妊娠 24 周和 80 名妊娠 28 周的孕妇进行血清样本检测。其中一半孕妇妊娠正常,另一半孕妇发生 SPTB。
在妊娠 24 周和 28 周的发生后续 SPTB 的孕妇中,有三种特定的来自α-胰蛋白酶抑制剂重链 4 蛋白的肽显著减少。最具区分度的肽的灵敏度为 65.0%,特异性为 82.5%;比值比为 8.8;95%置信区间为 3.1-24.8。将 3 种新型生物标志物与 6 种先前研究的生物标志物相结合,可将 28 周时的灵敏度提高到 86.5%,特异性为 80.6%。
通过血清蛋白质组学技术鉴定了三种新的 SPTB 血清标志物。使用这些新标志物与其他标志物的组合,可以在 SPTB 发生前数周识别出 SPTB 高危孕妇。